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Compare with a control solution prepared using 5.0mL of standard sodium chloride solution

A valid stability-indicating method must: Resolve the main peptide from all degradation products Detect impurities at low regulatory thresholds Accurately quantify impurities even in stressed samples Forced degradation samples are therefore essential during method development and validation for GLP-1 peptide drugs

doi: 10.1002/iub.186 3 KorkmazBCaugheyGHChappleIGauthierFHirschfeldJJenneDEet al

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Fue aprobado bajo el nombre comercial Egrifta por FDA para reduccin de lipodistrofia abdominal asociada con VIH